Celegence invites you to join us for the American Medical Device Summit on 18-19 October 2022. Setting the standard on how the industry should connect and exchange ideas, the American Medical Device Summit provides insights and strategies to enhance the professional development of executives involved in the design, product development, innovation, technology, and quality/ regulatory aspects of medical devices.
What: Lunch and Learn Roundtable Session on “Process and technology efficiency in post-market surveillance documentation for EU MDR”
When: Tuesday, October 18th at 1.05 PM – 2:05 PM CST
Where: Westin Chicago Lombard, Chicago, USA
How: Register Here
Why: Join this session to understand the impact of EU MDR in the medical device industry and learn how you can increase compliance and produce higher quality CER reports faster, by using dedicated technology.
Join the discussion with over 250 of your industry peers as they explore the challenges and opportunities in medical device innovation, regulatory harmonization, compliance, digital transformation and more. Hear first-hand case studies presented by the executive speaker faculty with extensive experience driving development and process strategy excellence. Walk away with strategic insights for industry, hospital networks and regulatory bodies to collaborate together to streamline processes, optimize development, design, decrease risk, improve speed to market, reduce costs and remain compliant in a rapidly evolving landscape. This October, we encourage you to join the AMD Summit for two days of thought-provoking content and exceptional networking.
Celegence is excited to be a sponsor at the American Medical Device Summit this year in Chicago, USA. Come together with other regulatory affairs professionals to discuss pressing regulatory topics and understand the impact EU MDR and increased harmonization has in the medical device Industry.
This session will be led by Celegence’s Medical Device Regulatory Specialist, Joseph-Richardson Larbi.